A68G (p.Ala68Gly) variant of FBN2 (Fibrillin-2)
A68G (p.Ala68Gly) in FBN2 (Fibrillin-2) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes population frequency data and structural context.
A68G (p.Ala68Gly) variant details
- p.Ala68Gly
- 1000Genomes rs62390671
- ESP rs62390671
- ExAC rs62390671
- TOPMed rs62390671
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Population evidence available
- Structural context available